7508-32-9

Usage

Uses

Used in Organic Chemistry:
(2-hydroxy-3,4-dimethoxyphenyl)(phenyl)methanone is used as a building block for the synthesis of various other compounds due to its versatile chemical structure and multiple functional groups.
Used in Pharmaceutical Industry:
(2-hydroxy-3,4-dimethoxyphenyl)(phenyl)methanone is used as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
(2-hydroxy-3,4-dimethoxyphenyl)(phenyl)methanone is used as a precursor in the production of agrochemicals, such as pesticides and herbicides, due to its reactivity and functional groups.
Used in Materials Science:
(2-hydroxy-3,4-dimethoxyphenyl)(phenyl)methanone is used in the development of new materials with specific properties, such as polymers and composites, for various applications in materials science.
It is important to handle (2-hydroxy-3,4-dimethoxyphenyl)(phenyl)methanone with care and follow proper safety protocols due to its potential health hazards and reactivity.

Upstream product

• 634-36-6 1,2,3-trimethoxybenzene 
• 98-88-4 benzoyl chloride 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 
• 1143-72-2 2,3,4-trihydroxybenzophenone 
• 186581-53-3 diazomethane 
• 623-11-0 1-methyl-4-nitrosobenzene 

Downstream Products

• 108837-10-1 6,7-dimethoxy-3-phenyl-benzofuran 
• 94709-11-2 2,3,4-trimethoxybenzophenone 
• 140665-35-6 5-chloro-2-hydroxy-3,4-dimethoxybenzophenone 
• 1143-72-2 2,3,4-trihydroxybenzophenone 
• 4646-78-0 2,5-dihydroxy-3,4-dimethoxy-benzophenone 

Relevant academic research and scientific papers

Hypolipidemic 1,4-benzothiazepine derivative

The invention is concerned with a novel hypolipidemic compound, which is of (3R,5R)-3-Butyl-3-ethyl-2,3,4,5-tetrahydro-7-methoxy-5-phenyl-1,4-benzothiazepin-8-ol 1,1-dioxide; or a salt, solvate, or physiologically functional derivative thereof, with processes for its preparation, pharmaceutical compositions containing it and with its use in medicine, particularly in the prophylaxis and treatment of hyperlipidemic conditions, such as athersclerosis.

Determination of the sequential order of acidity in a polyhydroxylated benzophenone series. Consequence on the oxidation reaction in relation to hepatotoxicity

The pKa values of successive acid-base equilibria involved in the pyrogallol ring ionisation of exifone, 2,3,4-trihydroxybenzophenone 1, and related methoxy derivatives were determined by UV-VIS absorption spectrometry and potentiometric titration.Due to strong intramolecular hydrogen bonding, the sequential order of acidity of the three hydroxy groups of 1 was found to be 4-OH > 3-OH > 2-OH.The polyhydroxylated benzophenones were oxidized to 3,4-quinone only in a narrow range of acidity in which the monoanionic 4-olate species predominated in solution.The attachment of an amino-alcohol residue resulted in the trapping of the transient 3,4-quinone and provided a convenient route to novel 1,4-benzoxazine derivatives.Cytotoxicity experiments in rat hepatocytes indicated that some of these compounds were significantly less toxic than the parent exifone.

Studies on uricosuric diuretics. III. Substituted 1,3-dioxolo[4,5-f]-1,2-benzisoxazole-6-carboxylic acids and 1,3-dioxolo[4,5-g]-1,2-benzisoxazole-7-carboxylic acids

A series of substituted 1,3-dioxolo[4,5-f]-1,2-benzisoxazole-6-carboxylic acids 13 and 1,3-dioxolo[4,5-g]-1,2benzisoxazole-7-carboxylic acids 14 were synthesized and evaluated for diuretic and uricosuric activities in rats. Most of the benzisoxazole deriv